N-acetylcysteine during critical neurodevelopmental periods prevents behavioral and neurochemical deficits in the Poly I:C rat model of schizophrenia

Schizophrenia is a chronic neurodevelopmental disorder with an inflammatory/prooxidant component. N-acetylcysteine (NAC) has been evaluated in schizophrenia as an adjuvant to antipsychotics, but its role as a preventive strategy has not been sufficiently explored. We aimed to evaluate the potential of NAC administration in two-time windows before the onset of symptoms in a schizophrenia-like maternal immune stimulation (MIS) rat model. Pregnant Wistar rats were injected with Poly I:C or Saline on gestational day (GD) 15. Three different preventive approaches were evaluated: 1) NAC treatment during periadolescence in the offspring (from postnatal day [PND] 35 to 49); 2) NAC treatment during pregnancy after MIS challenge until delivery (GD15–21); and 3) NAC treatment throughout all pregnancy (GD1–21). At postnatal day (PND) 70, prepulse inhibition (PPI) and anxiety levels were evaluated. In vivo magnetic resonance (MR) imaging was acquired on PND100 to assess structural changes in gray and white matter, and brain metabolite concentrations. Additionally, inflammation and oxidative stress (IOS) markers were measured ex vivo in selected brain regions. MIS offspring showed behavioral, neuroanatomical, and biochemical alterations. Interestingly, NAC treatment during periadolescence prevented PPI deficits and partially counteracted some biochemical imbalances. Moreover, NAC treatments during pregnancy not only replicated the beneficial outcomes reported by the treatment in periadolescence, but also prevented some neuroanatomical deficits, including reductions in hippocampal and corpus callosum volumes. This study suggests that early reduction of inflammation and prooxidation could help prevent the onset of schizophrenia-like symptoms, supporting the importance of anti-IOS compounds in ameliorating this disorder.


INTRODUCTION
Schizophrenia is a chronic neuropsychiatric disorder that affects more than 20 million people worldwide [1], with symptoms usually emerging in late adolescence or early adulthood [2].Despite its global impact, the etiology of schizophrenia remains elusive, although the significant involvement of neuroinflammation in its diverse pathophysiological domains has been widely recognized [3].In this context, drug-naïve first-episode psychotic (FEP) patients exhibit inflammatory abnormalities independent of medication use [4].Furthermore, impairments in the glutathione (GSH) system compromise N-methyl-D-aspartate (NMDA) receptor activity, suggesting that oxidative damage is also a relevant mechanism contributing to cognitive impairment [5].There is increasing evidence indicating an elevated risk of schizophrenia-related abnormalities resulting from neurodevelopmental defects caused by prenatal exposure to infections [6].These findings propose the presence of various abnormalities with closely interconnected mechanisms within the brains of these patients.Thus, environmental risk factors can impact neuroproliferation and synaptic pruning, which are essential for healthy brain development during early prenatal periods and adolescence, respectively [7].Consequently, these stages emerge as critical periods for the occurrence of high-risk abnormalities associated with subsequent neuropsychiatric conditions.Therefore, mitigating the impact of different environmental insults that may contribute to pathological neurodevelopmental imbalances could delay or prevent the onset of schizophrenia.Given the influential roles of adolescence and prenatal periods, both periods represent critical time windows for schizophrenia prevention [8].
Significant efforts have been made to develop effective strategies for predicting and preventing the transition to psychosis in high-risk patients [9].However, current findings are still far from reliable.The ideal strategy would involve identifying patients at high risk for psychosis and implementing a treatment that can prevent their pathological transition without side effects.Accordingly, N-acetylcysteine (NAC) has garnered significant attention due to its remarkable ability to modulate impaired molecular systems in various psychiatric disorders, including schizophrenia [10,11].NAC, an antioxidant agent, plays a primary role in promoting GSH synthesis, thereby helping to restore oxidative homeostasis and neurotransmitter signaling [12].With its low toxicity and minimal side effects profile [13], NAC has emerged as a promising candidate for preventive strategies in schizophrenia.
Previous preclinical studies have demonstrated some benefits of NAC treatment during adolescence as a preventive strategy [14,15].However, in clinical trials, NAC has only been evaluated as an adjuvant to antipsychotics [10], mainly due to the challenges associated with the early identification of high-risk patients.This suggests that earlier administration would be more appropriate.Notably, one study has already demonstrated the efficacy of a single injection of NAC following prenatal inflammation in three schizophrenia-like rat models [16].Nonetheless, this approach requires almost immediate and invasive intervention, posing challenges for translation into the clinical setting.Therefore, there is a need for more translational strategies to evaluate the preventive potential of NAC during the prenatal period.
In this study, our initial aim was to assess the potential preventive effects of NAC administration during periadolescence in a maternal immune stimulation (MIS) rat model of schizophrenia.Building upon the promising findings, we further investigated NAC treatment during pregnancy in two different time windows: starting from the immune challenge or throughout the entire pregnancy.Notably, this study represents the first attempt to tackle this topic comprehensively using structural magnetic resonance imaging (MRI), diffusion tensor imaging (DTI), and MR spectroscopy (MRS), enabling us to evaluate in vivo structural and metabolic changes after NAC treatment.Additionally, we examined alterations in behavior and measured inflammation/oxidative stress (IOS) biomarkers, providing a broad perspective of the various levels affected in this animal model.

MATERIALS AND METHODS Animals
A total of 156 male Wistar rats were housed in a temperature-and humidity-controlled vivarium, following a 12 h dark/light cycle, and provided ad libitum access to standard rodent chow and tap water.Three separate batches of randomized animals were used for the different studies conducted.In the study performed during the periadolescent period, 84 rats were included, 35 animals from 17 litters for behavior (15 NAC, 20 Saline) and 49 animals for imaging (26 NAC,23 Saline).In the study performed during the gestational period, 72 rats from 46 litters were included (48 NAC, 24 Saline).The sample size was estimated on previous studies [17][18][19].All experimental animal procedures were conducted according to European Communities Council Directive 2010/63/EU and ARRIVE guidelines [20] and approved by the Ethics Committee for Animal Experimentation of Hospital Gregorio Marañón.
NAC treatment during gestation: NAC (500 mg/kg, Sigma-Aldrich) was administered in fresh drinking water (VH) during two different time windows: 1) from the immune challenge (GD15) until delivery (NAC7d); and 2) throughout the entire gestation (NAC21d).The study comprised six groups based on the experimental factors: phenotype (MIS, Saline) and treatment (VH, NAC7d, NAC21d). Figure 1A illustrates the design of the study.

Behavioral studies
Behavioral studies were conducted between PND70-80 (early adulthood).Sensorimotor gating was assessed in all animals, while anxiety was measured specifically in the gestational study.
Elevated plus maze test.At PND80, anxiety levels were assessed using the elevated plus maze (EPM) test.The maze (Cibertec, Spain) consisted of two open arms and two enclosed arms at right angles (arms: 50 cm long, 40 cm high, 10 cm wide) raised 50 cm above the floor.Animals were placed in the center of the EPM, facing an open arm, and allowed to explore for 5 min.All experiments were recorded.The maze was cleaned between each animal using a 0.1% acetic acid solution.The total time spent in the open and closed arms, and the number of head dippings, were quantified.
In vivo magnetic resonance studies.Animals were scanned during adulthood (PND 100-120) using a 7-Tesla Biospec 70/20 scanner (Bruker, Germany) under sevoflurane anesthesia (3% induction, 1.5% maintenance in 100% O 2 ).Rat-specific volume and surface coils were used.All animals were scanned for structural changes in gray matter.Diffusion tensor imaging (DTI) and spectroscopy studies were only performed on the animals participating in the gestational study (Supplementary Fig. 1).
Structural MRI imaging: Acquisition and reconstruction protocols were published elsewhere [18,19].Briefly, T2-weigthed Spin Echo (SE) coronal images were acquired with TE of 33 ms, TR of 3.732 ms and 0.4 mm in thickness.The matrix size was 256×256 pixels, covering a FOV of 3.5×3.5 cm 2 .The artifacts caused by the surface coil were corrected.Seven ROIs (PFC, whole cortex, hippocampus, cerebellum, ventricles, corpus callosum, and whole brain) were manually segmented [21], by two blinded operators, with in-depth anatomical knowledge, to reduce operator variability.This manual approach was used due to its robustness, as brain atlas-based segmentations for rodents still have some deficiencies in automated segmentation [22].
DTI study: Structural changes in white matter were evaluated using DTI.MR spectroscopy: 1 H-MRS images were acquired using a PRESS monovoxel sequence in the PFC and hippocampus, with the following parameters: TR of 2500 ms, TE of 16.5 ms, 2,048 acquisition points, 128 averages, bandwidth of 3301.06Hz, and voxel size of 1.5 mm 3 , adjusted to the anatomical structure.An unsuppressed water signal was used as an internal reference for quantification.In vivo 1 H-MRS spectra were analyzed using LCModel (Version 6.2-0U, S.W.Provencher) [23], considering only metabolites with a Cramer-Rao Lower Bound (CRLB) of less than 20%.Additionally, metabolites with overlapping resonances were presented as the combined sum of both species.
Lipid peroxidation: The Thiobarbituric Acid Test for MDA was performed as described by Das and Ratty [25].
NRF2 activity: A commercial ELISA-based kit (600590, Cayman Chemical, Estonia) was used on nuclear extracts of tissue samples, following the manufacturer's instructions.

Statistical analyses
Normality and homoscedasticity were assessed by Shapiro-Wilk's and Levene's tests, respectively.Normal and homoscedastic variables were analyzed using a two-way ANOVA followed by a Bonferroni post hoc test.For the PPI results, a repeated-measures (RM) ANOVA was employed, considering phenotype, treatment, and prepulse intensity as factors.Nonnormal and non-homoscedastic variables were analyzed using the Kruskal-Wallis (KW) test and Dunn's post hoc test.A p value < 0.05 was considered statistically significant for all analyses.Statistical analyses were performed using SPSS (IBM SPSS Statistics 20, Spain), and graphic representations were generated using GraphPad Prism (v8, GraphPad Software, San Diego, CA, USA).Data are presented as mean ± SEM.

RESULTS
Tables 1 and 2 provide a comprehensive overview of the results from the statistical analyses investigating the effects of NAC during periadolescence and pregnancy, respectively, for each of the conducted experiments.

Behavioral studies
Prepulse inhibition of the startle reflex.The PPI assesses deficits in sensorimotor gating, a common symptom in schizophrenia, by evaluating the suppression of an acoustic startle reflex to an intense stimulus when pre-exposed to a weak stimulus.We confirmed the presence of these deficits in our model, as both the periadolescence and gestational MIS-VH groups exhibited a significant PPI reduction at 80 dB and 86 dB (vs.Saline-VH group).In the periadolescence study, the RM-ANOVA revealed a significant prepulse effect (p < 0.001), an interaction between MIS and treatment (p < 0.05), and a three-way interaction (prepulse, MIS, and NAC) (p < 0.05) (Fig. 1C).Post hoc tests indicated that NAC did not significantly alter PPI values in the VH animals, but it prevented the PPI reduction in the MIS-offspring (vs.MIS-VH group).In the gestational study, the RM-ANOVA revealed significant effects of MIS (p < 0.01), NAC treatment (p < 0.01), and prepulse (p < 0.001) (Fig. 1D).Post hoc tests showed that NAC7d did not significantly improve PPI in the MIS-offspring, whereas NAC21d fully prevented this deficit (vs.MIS-VH group).
Elevated plus maze.The EPM (Fig. 1E) was used to evaluate anxiety levels in this model.Consistent with expectations, the MIS-VH animals spent more time in the closed arms and less time in the open arms compared to the Saline-VH rats, indicating higher anxiety levels.Additionally, the MIS-VH group exhibited a significant reduction in the number of head-dippings (p < 0.001).Importantly, both the NAC7d and NAC21d treatments completely prevented these deficits in the MIS-offspring.

MRI studies
In adulthood, T2-weighted images were acquired to evaluate changes in regional volumetry.Moreover, DTI and metabolite content data were obtained in the gestational approach.
Volumetry.Six brain regions were segmented on T2-weighted images and analyzed using a regions-of-interest (ROIs) approach.In the periadolescence study (Fig. 2A.1), the MIS-VH animals exhibited significant ventricular enlargement and reduced volume in the hippocampus and corpus callosum (vs.Saline-VH rats) (p < 0.01 in all cases), although none of these deficits were prevented by NAC.In the gestational study (Fig. 2A.2), the MIS-VH animals displayed reduced volume in the hippocampus, cerebellum, and nearly significant reduction in the corpus callosum (p = 0.06), along with ventricular enlargement (p < 0.05).In this case, both NAC7d and NAC21d prevented the hippocampal and corpus callosum deficits.Furthermore, we observed a trend towards the prevention of volumetric abnormalities in the ventricles (p = 0.07) and cerebellum (p = 0.07) by NAC7d and NAC21, respectively.Finally, the Saline-NAC7d offspring exhibited increased cortical volume (p < 0.01).

MRS.
The uni-voxel spectroscopy data did not reveal statistically significant differences for any of the metabolites.However, a noticeable trend indicating a time-dependent effect of NAC was observed for choline in the PFC (Fig. 2C.1) and hippocampus (Fig. 2C.2), as well as for N-acetyl aspartate in the PFC.

IOS determinations
Our ex vivo analyses (Figs.3-4) of brain tissue confirmed the presence of a region-dependent pro-inflammatory/pro-oxidant environment in the MIS-offspring.Importantly, NAC treatments partially and differentially prevented these abnormalities.

Periadolescence study
In the PFC, the ANOVA analysis showed a significant effect of MIS in iNOS (Fig. 3A) as well as on CAT, MDA, GSH total , GSH free , and GSSG.Interestingly, there was a great preventive effect of NAC on iNOS and KEAP1 in the MIS-offspring.In the hippocampus (Fig. 3B), no significant effect of MIS was observed, but an effect of NAC was found in COX2 and KEAP1.In the amygdala (Fig. 3C), a significant MIS effect was found in iNOS, COX2, KEAP1, and HO1.Furthermore, NAC significantly reduced COX2 expression while increasing the expression of HO1, NQO1, NRF2, and SOD.In the caudate-putamen, a significant MIS effect was observed in iNOS, GSH total , and GSSG, while NAC increased HO1 expression and reduced NRF2 and CAT levels.
Gestational study.In the PFC (Fig. 4A), the MIS-offspring exhibited a significant increase in iNOS levels, which were effectively prevented by NAC in both time-windows.Furthermore, NAC21d increased MDA levels and reduced NRF2 levels.In the hippocampus (Fig. 4B), COX2 activity significantly increased due to MIS challenge, although no modulation was observed by NAC.Instead, NAC7d reduced iNOS expression and increased CAT activity, while NAC21d modulated iNOS, CAT, and NQO1.Post-hoc analyses revealed a significant increase in NQO1 activity in MIS-NAC21d animals (p < 0.05) and in CAT activity in Saline-NAC21d animals (p < 0.01).In the amygdala (Fig. 4C), MIS-challenge led to increased iNOS and COX2 activity and reduced NRF2 expression.NAC7d showed a significant effect in iNOS, COX2, and GSSG, whereas NAC21d modulated iNOS, COX2, NQO1, and CAT.Interestingly, NAC7d prevented the excessive expression of COX2 in the MIS-offspring (p < 0.001), thereby reducing its proinflammatory consequences.Additionally, NAC21d increased the levels of the antioxidant biomarker NQO1 (p < 0.05).Lastly, in the caudateputamen, MIS increased COX2 activity and reduced MDA, KEAP1, and GPx.The ANOVA analyses revealed an effect of NAC7d on KEAP1 and NQO1, increasing their levels in MIS-offspring, and an effect of NAC21d modulating COX2, CAT, and GSSG.

DISCUSSION
This study explores the potential of NAC to prevent the development of schizophrenia-like deficits in the MIS model.NAC treatment was administered during two different time windows: 1) periadolescence, before the onset of initial symptoms, and 2) gestation, aiming to mitigate the risk of neurodevelopmental abnormalities in prenatal offspring associated with heightened IOS.In both cases, NAC successfully prevented certain neuroanatomical, biochemical, and behavioral deficits in the MIS-offspring, with the gestational treatment showing particular efficacy in early intervention.Although several studies have explored the potential therapeutic effects of NAC and other anti-IOS drugs in the MIS model, only a limited number have focused on preventive strategies, particularly during the periadolescent period.Among them, various compounds, such as minocycline [19,26], omega-3 fatty acids (ω−3) [18], phosphodiesterase-9 inhibitors [27], or even antipsychotic or antidepressant drugs [28,29] have been administered during periadolescence, with variable result.In this regard, we have recently showed that ω−3 [18] and mangiferin [30] treatments during adolescence were effective in the prevention of behavioral deficits in PPI and some of the volumetric and metabolic deficits seen in this model.Furthermore, we have demonstrated that minocycline-treatment during adolescence partially counteracts volumetric abnormalities and IOS deficits in the MIA model, likely via iNOS and Nrf2-ARE pathways, also increasing the expression of cytoprotective enzymes [31].On the other hand, the gestational approach has only been explored in two studies.The first demonstrated that NAC treatment during pregnancy was useful in preventing the hippocampal reduction and hippocampal-based memory impairments, along with a partial prevention of gut microbiota deficits observed in MIS-offspring [32].The second evaluated NAC and omega-3 fatty acids during gestation from the immune insult to the delivery [33].In contrast to our results, Edemann-Callesen et al. reported only a partial relief in behavior and prevention of microglial activity, as well as enlargement of lateral ventricles in the adult offspring from dams treated with omega-3 fatty acids, evidencing the necessity for further multiscale research.In this line, it is worth noting that there have been no further studies evaluating the effects of NAC administration specifically throughout the entire pregnancy period in this model, including both in vivo and ex vivo techniques, which makes this study of great relevance.At the biochemical level, we examined the concentration and activity of various markers related to IOS in four brain regions known to be implicated in schizophrenia [7,34] and affected in the MIS model [18,19].Our findings revealed prominent alterations in the PFC and amygdala in the MIS-offspring.Remarkably, NAC treatment demonstrated a preventive effect on these alterations, particularly in the amygdala.The amygdala plays a crucial role in processing fear and threat-related stimuli and has been widely associated with the development of anxiety disorders [35].Hence, the beneficial antioxidant properties of NAC during pregnancy may contribute to the complete prevention of anxietylike behaviors observed in the MIS-offspring.
One of the consistently altered markers of IOS in the MIS model is iNOS.This isoform of NOS is known to induce cytotoxicity by promoting the production of nitric oxide (NO) in various cell systems.Activation of iNOS may occur in PolyI:C-treated dams when PolyI:C binds to TLR-3 receptors, subsequently activating the NF-κB pathway [36].These changes, probably mediated by the interaction between microglia and neurons during neurodevelopment [37], may persist and contribute to the long-term imbalance in IOS observed in this animal model.Furthermore, iNOS has also been implicated in different stages of the disorder [38].In our study, we observed an increase in iNOS in the MIS-offspring, and importantly, prenatal and periadolescence NAC treatment effectively prevented this alteration.
Moreover, we observed significant differences in the expression of COX2 and SOD in the amygdala during the periadolescence study.The MIS-offspring exhibited increased expression of SOD and decreased expression of COX2, which aligns with the inverse correlation proposed by Lee et al [39].
Additionally, we investigated the antioxidant response element (ARE) proteins, namely HO1 and NQO1, which are known to play a crucial role in cellular antioxidant.Moreover, both HO1 and NQO1 have been reported to be altered in the MIS model [18,19].Although we did not observe significant differences in HO1 and NQO1 expression in this model, we did find an impact of NAC treatment on the enzymatic activity of these proteins in the amygdala, particularly when NAC was administered during periadolescence and throughout pregnancy.Similar trends were observed in the PFC, although they did not reach statistical significance.These findings support the notion of an oxidative imbalance within the amygdala and indicate the involvement of HO1 and NQO1 in the preventive effects of NAC.Both proteins are activated through the NRF2 pathway, which involves the dissociation of NRF2 from KEAP1, its translocation into the nucleus, and subsequent binding to target transcription factors [40].Interestingly, we observed significant differences in KEAP1 levels in MIS-offspring, and these differences were largely prevented by NAC treatments.Nevertheless, we did not find any differences in NRF2 levels.It is possible that the activation of HO1 and NQO1 occur through an alternative pathway that is less commonly observed, potentially explaining this seemingly contradictory results [41].In any case, our study demonstrates the ability of NAC during periadolescence and, especially, during gestation, to prevent some of the IOS deficits observed in the PFC and amygdala of the MIS model.
At the neuroanatomical level, MIS-offspring did not show the anticipated cortical volume reduction.However, a significant decrease in hippocampal volume was observed in MIS-offspring, and this reduction was effectively prevented by both prenatal NAC treatments, but not by periadolescence treatment.Hippocampal volume reduction is a known characteristic in individuals with schizophrenia and has been associated with various clinical outcomes in this disorder [42].Interestingly, in our study, this reduction in hippocampal volume was not accompanied by an increase of IOS in this region.This suggests that the symptomatology observed in this animal model may be more closely related to an exacerbated increase in IOS rather than anatomical alterations (i.e., PPI is modulated by the corticostriatal-pallidum-thalamic (CSPT) circuitry involving the PFC) [43].Furthermore, MIS-offspring exhibited ventricular enlargement, an alteration that has also been associated with schizophrenia [44] and other neurodevelopmental disorders [45], and has been described in this animal model [17][18][19].While periadolescent NAC administration did not lead to a reduction in ventricular volume in MIS animals, a non-significant improvement was observed when the treatment was administered during the final seven days of gestation, indicating that earlier NAC treatment yields more favorable outcomes.
The cerebellum is another structure that may potentially benefit from the administration of NAC.Reduced cerebellar volume has  been observed in patients with schizophrenia, and these alterations have been associated with the onset of positive symptoms [46], although it is worth noting that this reduction has also been attributed to the side effects of antipsychotics [17].In our study, although NAC treatment during periadolescence did not have an impact on cerebellar volume, the administration of NAC throughout gestation nearly counteracted this reduction.These findings suggest that the prenatal approach of NAC treatment may have some preventive potential in addressing cerebellar-related deficits in schizophrenia.
Regarding white matter changes, we found a reduction in corpus callosum volume in MIS-offspring, which is consistent with previous studies demonstrating a generalized decrease in white matter volume [47] in individuals with schizophrenia.This alteration is associated with impaired connectivity between the two cerebral hemispheres.Interestingly, while NAC treatment during periadolescence did not prevent this deficit in MIS-offspring, both prenatal treatments completely prevented the reduction in corpus callosum volume.In addition to assessing volumetric changes, we also examined white matter alterations in the corpus callosum, PFC, and hippocampus using DTI.Surprisingly, we detected a significant increase in FA in the corpus callosum, and this increase was fully prevented by both NAC treatments during pregnancy.These findings contrast with clinical reports indicating reduced FA and MD in patients with schizophrenia and adolescents with early-onset psychosis [48].Currently, we do not have an explanation for this unexpected finding.One possibility could be related to fiber compaction in the corpus callosum, leading to volume reduction and subsequently an increase in FA in the MIS model.Nevertheless, it is important to note that this increase in FA does not correlate with the corpus callosum size, as we observed the same volume reduction in both the animal model and the human disorder.
In terms of brain metabolic changes, abnormalities in the levels of glutamate + glutamine (neurotransmitter and precursor) and N-Acetyl Aspartate + glutamic acid (NAA + NAAG; neuronal viability) in the PFC have been associated with schizophrenia in patients with psychotic disorders and individuals at ultra-high risk for psychosis [49].These abnormalities have also been implicated in the progression of the pathology [50].In the MIS model, our study is the first report to tackle this issue.We did not observe significant differences in metabolite concentrations following MIS challenge.However, there was a trend towards increased NAA + NAAG and choline levels in the Saline and MIS-offspring treated with NAC during pregnancy.This potential increase in NAA + NAAG levels is particularly interesting and promising, as reduced NAA levels have been associated with poor disease progression in schizophrenia [50].
In terms of behavioral tests, we were able to confirm the presence of a deficit in PPI and increased anxiety levels in MISoffspring, which is consistent with findings from other studies [51,52].Importantly, all NAC treatments, particularly the prenatal approaches, effectively prevented these deficits in both PPI and anxiety.Deficits in PPI and anxiety are well-documented in clinical studies [53] and preclinical research [54].Specifically, PPI deficits have been associated with impairment in the PFC [55], which was also altered in terms of IOS in our study.Furthermore, the cerebellum, another region affected in our MIS animals, has been implicated in auditory processing impairment [56], which could be involved in the observed deficits in response to acoustic stimuli in this behavioral test.
Overall, the three NAC treatment approaches effectively prevented behavioral deficits in sensorimotor gating and anxiety, as well as some of the biochemical alterations in the brain.However, the impact on neuroanatomical anomalies was not consistent across the different approaches.Treatment with NAC during periadolescence had limited effects on brain anatomy, whereas administration during pregnancy showed more promising results, possibly due to its ability to intervene earlier in the developmental process.It is worth noting that neuroanatomical abnormalities have been reported prior to the onset of symptoms in schizophrenia [57].Therefore, initiating therapeutic interventions with a safe compound during pregnancy may have the potential to prevent long-term deficits associated with IOS dysfunction in offspring, by addressing neurodevelopmental abnormalities at an early stage.
This study has several limitations that should be acknowledged.Firstly, the study was conducted exclusively in male-offspring.It is known that the effects of MIS differ between males and females in terms of functional and morphological changes [58].Additionally, the onset of schizophrenia symptoms occurs later in women than in men.However, exploring these gender differences was beyond the scope of our current study, and focusing on male offspring allowed us to establish common therapeutic and sampling windows.Nonetheless, it is important to extend our approaches to include female offspring in future investigations.Secondly, a modification to the acquisition protocol in the MRS study, such as using a larger voxel size and increasing the number of repetitions, could have potentially yielded stronger and more robust results by improving the signal-to-noise ratio.Thirdly, it should be noted that the periadolescence approach did not include studies on anxiety, DTI, and MRS, as these aspects were incorporated into the gestational approach based on the promising results obtained during periadolescence, This expansion of the experimental battery allowed for a more comprehensive assessment of the model.Fourthly, despite the sample size of each group seems to be adequate for the purposes of this study, we acknowledge that MRI volumetric results could have benefited from a limited increase in the number of animals included in each group.Finally, we must acknowledge that no corrections for multiple comparisons were performed.This decision is justified by the exploratory nature of the study and by the fact that most measurements were decided a priori, based on the results of previous studies.In addition, these methods assume independency of the tests, which may not be true in our complex dataset due to potential interdependencies between markers and brain regions examined, which could potentially blur true associations or patterns.However, we recognize the inherent bias associated with this approach that may lead to a certain degree of Type I error.Consequently, interpretation of these results should be taken with caution and emphasize the need for replication studies to further validate these findings.
In summary, treatment with NAC during both gestation and periadolescence effectively prevented behavioral deficits and various biochemical alterations in the MIS model.Additionally, prenatal administration of NAC demonstrated the ability to prevent some of the neuroanatomical anomalies observed in the MIS model.These findings suggest that early therapeutic interventions hold promise in reducing the prenatal IOS status and decreasing the severity and risk of developing schizophrenia-like deficits in offspring.
sequences were acquired, with TR of 2000 ms, TE of 26.55 ms, three repetitions, diffusion gradients applied in 27 directions (b value = 1000 s/ mm 2 ), 35 slices, 0.4 mm thickness, matrix size of 128 × 128 voxels, and FOV of 35 × 35 mm.Fractional anisotropy (FA) and mean diffusivity (MD) values were determined in the corpus callosum, PFC, and hippocampus.

Table 1 .
Statistical data of NAC-related effects during periadolescence on brain volumetry (A) and the expression of inflammatory and oxidative (IOS) markers (B).
DTI. Differences in FA and MD were assessed through ROI analyses of the DTI images.The MIS-VH animals exhibited an increase in FA in the corpus callosum (p < 0.01, vs. Saline-VH), which was prevented by both NAC7d and NAC21d (p < 0.001) (Fig.2B.1).No significant differences in FA were observed in other ROIs.Conversely, significant effects of NAC7d and NAC21d were observed (p < 0.05), restoring MD values in the prefrontal cortex (PFC) and hippocampus (Fig.2B.2).

Table 2 .
Statistical data of NAC-related effects during pregnancy on anxiety (A), brain volumetry (B), brain DTI (C), brain MRS (D) and the expression of inflammatory and oxidative (IOS) markers (E).